(Q39086510)

8 September 2017

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study (English)

1 reference

8 September 2017

1 reference

18

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8 September 2017

Ramu Elango

6

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Rachel A Gibson

object named as

Rachel A Gibson

16

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Paul M. Matthews

object named as

Paul M Matthews

14

0 references

M M Hulihan

1

object named as

Hulihan MM

1 reference

8 September 2017

2

Ishihara-Paul L

1 reference

8 September 2017

3

Kachergus J

1 reference

8 September 2017

4

Warren L

1 reference

8 September 2017

Rim Amouri

5

1 reference

8 September 2017

Rab K Prinjha

7

1 reference

8 September 2017

Ruchi Upmanyu

8

1 reference

8 September 2017

Mounir Kefi

9

1 reference

8 September 2017

Mourad Zouari

10

1 reference

8 September 2017

Samia Ben Sassi

11

1 reference

8 September 2017

Samia Ben Yahmed

12

1 reference

8 September 2017

Ghada El Euch-Fayeche

13

1 reference

8 September 2017

Lefkos T Middleton

15

1 reference

8 September 2017

Fayçal Hentati

17

1 reference

8 September 2017

language of work or name

English

0 references

publication date

6 June 2008

1 reference

8 September 2017

1 reference

8 September 2017

7

1 reference

8 September 2017

591-594

1 reference

8 September 2017

7

1 reference

Genetics of Parkinson disease: paradigm shifts and future prospects.

8 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Evaluation of LRRK2 G2019S penetrance: Relevance for genetic counseling in Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Genetic characterization and origin of Tunisian Berbers

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

What features improve the accuracy of clinical diagnosis in Parkinson's disease: A clinicopathologic study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Parkinsonism: onset, progression, and mortality

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

A New Method for Measuring Daytime Sleepiness: The Epworth Sleepiness Scale

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Epidemiology of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Clinical and genetic study of familial Parkinson's disease in Tunisia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

Parkinsonism, Lrrk2 G2019S, and tau neuropathology

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2808%2970116-9

7 January 2021

10.1016/S1474-4422(08)70116-9

Identifiers

DOI

1 reference

8 September 2017

1 reference